Gene Gene information from NCBI Gene database.
Entrez ID 54861
Gene name SNF related kinase
Gene symbol SNRK
Synonyms (NCBI Gene)
HSNFRK
Chromosome 3
Chromosome location 3p22.1
Summary SNRK is a member of the sucrose nonfermenting (SNF)-related kinase family of serine/threonine kinases (Kertesz et al., 2002 [PubMed 12234663]).[supplied by OMIM, Apr 2009]
miRNA miRNA information provided by mirtarbase database.
794
miRTarBase ID miRNA Experiments Reference
MIRT022051 hsa-miR-128-3p Microarray 17612493
MIRT031002 hsa-miR-21-5p Microarray 18591254
MIRT041578 hsa-miR-193b-3p CLASH 23622248
MIRT721142 hsa-miR-4422 HITS-CLIP 19536157
MIRT721141 hsa-miR-154-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000287 Function Magnesium ion binding IDA 12234663
GO:0000287 Function Magnesium ion binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612760 30598 ENSG00000163788
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRH2
Protein name SNF-related serine/threonine-protein kinase (EC 2.7.11.1) (SNF1-related kinase)
Protein function May play a role in hematopoietic cell proliferation or differentiation. Potential mediator of neuronal apoptosis.
PDB 5YKS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 16 269 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in hematopoietic progenitor cells and leukemic cell lines. Weakly expressed in the testis. {ECO:0000269|PubMed:12234663, ECO:0000269|PubMed:8654423}.
Sequence
MAGFKRGYDGKIAGLYDLDKTLGRGHFAVVKLARHVFTGEKVAVKVIDKTKLDTLATGHL
FQEVRCMKLVQHPNIVRLYEVIDTQTKLYLILELGDGGDMFDYIMKHEEGLNEDLAKKYF
AQIVHAISYCHKLHVVHRDLKPENVVFFEKQGLVKLTDFGFSNKFQPGKKLTTSCGSLAY
SAPEILLGDEYDAPAVDIWSLGVILFMLVCGQPPFQEANDSETLTMIMDCKYTVPSHVSK
ECKDLITRMLQRDPKRRASLEEIENHPWL
QGVDPSPATKYNIPLVSYKNLSEEEHNSIIQ
RMVLGDIADRDAIVEALETNRYNHITATYFLLAERILREKQEKEIQTRSASPSNIKAQFR
QSWPTKIDVPQDLEDDLTATPLSHATVPQSPARAADSVLNGHRSKGLCDSAKKDDLPELA
GPALSTVPPASLKPTASGRKCLFRVEEDEEEDEEDKKPMSLSTQVVLRRKPSVTNRLTSR
KSAPVLNQIFEEGESDDEFDMDENLPPKLSRLKMNIASPGTVHKRYHRRKSQGRGSSCSS
SETSDDDSESRRRLDKDSGFTYSWHRRDSSEGPPGSEGDGGGQSKPSNASGGVDKASPSE
NNAGGGSPSSGSGGNPTNTSGTTRRCAGPSNSMQLASRSAGELVESLKLMSLCLGSQLHG
STKYIIDPQNGLSFSSVKVQEKSTWKMCISSTGNAGQVPAVGGIKFFSDHMADTTTELER
IKSKNLKNNVLQLPLCEKTISVNIQRNPKEGLLCASSPASCCHVI
Sequence length 765
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs17075517 RCV005903483
Clear cell carcinoma of kidney Benign rs17075517 RCV005903484
Colon adenocarcinoma Benign rs17075517 RCV005903480
Hepatocellular carcinoma Benign rs17075517 RCV005903481
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Colonic Neoplasms Inhibit 22874833
Colorectal Neoplasms Inhibit 22874833
Inflammation Associate 28722495
Ovarian Neoplasms Associate 28722495